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The advent of three-dimensional (3D) bioprinting offers a feasible approach to construct complex structures for soft tissue regeneration. Carboxymethyl cellulose (CMC) has been emerging as a very promising biomaterial for 3D bioprinting. However, due to the inability to maintain the post-printed stability, CMC needs to be physically blended and/or chemically crosslinked with other polymers. In this context, this study presents the combination of CMC with xanthan gum (XG) and hyaluronic acid (HA) to formulate a multicomponent bioink, leveraging the printability of CMC and XG, as well as the cellular support properties of HA. The ionic crosslinking of printed constructs with iron(III) via the metal-ion coordination between ferric cations and carboxylate groups of the three polymers was introduced to induce improved mechanical strength and long-term stability. Moreover, immortalized human epidermal keratinocytes (HaCaT) and human foreskin fibroblasts (HFF) encapsulated within iron-crosslinked printed hydrogels exhibited excellent cell viability (more than 95%) and preserved morphology. Overall, the presented study highlights that the combination of these three biopolymers and the ionic crosslinking with ferric ions is a valuable strategy to be considered for the development of new and advanced hydrogel-based bioinks for soft tissue engineering applications. [ABSTRACT FROM AUTHOR]

Poor interfacial contact between solid‐state electrolytes and electrodes limits high‐voltage performance of solid‐state lithium batteries. A new gel electrolyte is proposed via in‐situ polymerization, incorporating fluoroethylene carbonate (FEC) solvent and ionic liquid1‐butyl‐1‐methylpiperidinium bis(trifluoromethylsulfonyl)imide (PP14TFSI). This combination synergistically enhances Li ion transport, achieving a transfer number of 0.58 and improved electrochemical performance. FEC protects the Al current collectors from LiPF6 corrosion and promotes a protective interfacial layer formation. PP14TFSI improves interfacial contact and provides stable components. An interface layer of fluorine and nitrogen composites forms, preventing side reactions. LiCoO2||PPE||Li cell exhibits robust cycling stability at 4.45 V, retaining ~80 % capacity after 200 cycles at room temperature with 0.2 C and 1 C rates, showing increased coulombic efficiency. NCM811||PPE||Li cell also displays exceptional cycling. In‐situ polymerization and FEC‐ionic liquid coordination enable high‐voltage solid‐state lithium metal batteries for practical use. [ABSTRACT FROM AUTHOR]

The application of solar steam generation in seawater desalination is an effective way to solve the shortage of fresh water resources. At present, many kinds of photothermal conversion materials have been developed and used as evaporators in seawater desalination. However, some evaporators need additional thermal insulation or water supply devices to achieve efficient photothermal conversion. In addition, their complex, time consuming and no scalable preparation process, high cost of raw materials and poor salt resistance hinder the practical application of these evaporator. Owing to its distinctive nanoporous structure, diatomite as fossilized single-cells algae diatoms is a promising natural silica-based material for seawater desalination. They are taken from sea and that makes true sense to use them in the sea. Herein, we report the first example of synthesis robust three-dimensional (3D) natural-diatomite composite by assembling polyaniline nanoparticles covered diatomite into the polyvinyl alcohol pre-treated melamine foam frameworks and demonstrate its application as new evaporator for seawater desalination. The porous framework does not only improve the sunlight scattering efficiency, but also offer large network of channels for water transportation. The inherent mechanism behind salt desalination process involves the absorption of water molecules on the surface of the internal silica micro-nano pores, and evaporation under the heat induced by the polyaniline absorbed sunlight. Meanwhile, the metal ions are segregated by many available pores and channels to achieve the self-desalting effect. The developed evaporator possesses the superiority of multi-stage pore structure, strong hydrophilicity, low thermal conductivity, excellent light absorption, fast water transportation and salt-resistant crystallization as well as good durability. The evaporation rate without an additional device is found to be 1.689 kg m-2 h-1 under 1-Sun irradiation, and the energy conversion efficiency is as high as 95%. This work creates a platform and develops the prospect of employing green and sustainable natural-diatomite composite evaporator for practical applications of seawater desalination. [ABSTRACT FROM AUTHOR]

Curcumin (Cur) is an acidic polyphenol with some effects on α‐glucosidase (α‐Glu), but Cur has disadvantages such as being a weak target, lacking passing the blood–brain barrier and having low bioavailability. To enhance the curative effect of Cur, the hybrid composed of ZnO nanoparticles decorated on rGO was used to load Cur (ZnO@rGO‐Cur). The use of the multispectral method and enzyme inhibition kinetics analysis certify the inhibitory effect and interaction mechanism of ZnO@rGO‐Cur with α‐Glu. The static quenching of α‐Glu with both Cur and ZnO@rGO‐Cur is primarily driven by hydrogen bond and van der Waals interactions. The conformation‐changing ability by binding to the neighbouring phenolic hydroxyl group of Cur increased their ability to alter the secondary structure of α‐Glu, resulting in the inhibition of enzyme activity. The inhibition constant (Ki, Cur > Kis,ZnO@rGO‐Cur) showed that the inhibition effect of ZnO@rGO‐Cur on α‐Glu was larger than that of Cur. The CCK‐8 experiments proved that ZnO@rGO nanocomposites have good biocompatibility. These results suggest that the therapeutic potential of ZnO@rGO‐Cur composite is an emerging nanocarrier platform for drug delivery systems for the potential treatment of diabetes mellitus. [ABSTRACT FROM AUTHOR]